Lead operational delivery of clinical programs ensuring quality, speed, and efficiency. Collaborate with cross-functional teams in a biotechnology setting to bring innovative medicines to patients.
Responsibilities
Lead the operational delivery of complex clinical programs, ensuring studies are executed with quality, speed, and efficiency
Provide strategic input into study planning and design, anticipate risks, and partner closely with cross-functional and local teams to align execution with program strategy, timelines, and budgets
Provide strategic input on study design, country selection, enrollment, diversity, and patient-centric approaches
Identify and mitigate delivery risks to maintain progress and performance
Drive consistent, high-quality operational practices across assigned programs
Line-manage and develop Study Delivery Leads with clear objectives and accountability
Manage program-level budgets, vendors, and forecasting while embedding lessons learned and continuous improvement
Oversee program-level issues, risks, and escalations to ensure timely resolution
Partner cross-functionally to align priorities, resources, and execution plans
Requirements
Degree educated
Clinical trial execution experience and previous people leadership managing teams, projects, resources or directing the allocation of resources
Previous experience in life sciences or a related field, including biopharmaceutical clinical research.
Experience working with or overseeing clinical research vendors (e.g., CROs, central labs, imaging).
Strong experience managing multiple teams / direct reports across multiple geographies
Benefits
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits
Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Job title
Associate Director – Global Clinical Program Management
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